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A multimag that has more than one magnesium

Primary carnitine deficiency (PCD) is an autosomal recessive disorder characterized by a lack of plasma membrane carnitine transport owing to a shortcoming in the OCTN2 carnitine transporter

However, most patients do not exhibit specific symptoms in the early stages of OC and CA125 has limited sensitivity and specificity for early cancer detection (Liu et al., 2020)

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The results have also illustrated that the protein expression of ACSL4 NOX4 and COX2 was markedly reduced, while the level of GPX4 and FTH was notably elevated in KTC-1-shFTO in comparison with that of the vector group ( Figure 7D )